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Publication numberUS3004863 A
Publication typeGrant
Publication dateOct 17, 1961
Filing dateOct 4, 1960
Priority dateOct 4, 1960
Publication numberUS 3004863 A, US 3004863A, US-A-3004863, US3004863 A, US3004863A
InventorsJr Charles Louis Gray, Dettrc Robert Harold
Original AssigneeDu Pont
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Process for increasing the scratch resistance of glass
US 3004863 A
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Description  (OCR text may contain errors)

United States Patent r 3,004,863 PROCESS FOR INCREASWG THE SCRATCH RESISTANiIE 0F GLASS Charles Louis Gray, Jr., Wilmington, and Robert Hwold Dettre, Brandywine Hundred, DeL, assignors to E. I. du Pont de Nemours and Company, Wilmington, Del, a corporation of Delaware No Drawing. Filed Oct. 4, 1960, Ser. No. 60,291 8 Claims. (Cl. 117-94) This invention relates to an improved process for increasmg the scratch resistance of glass bodies.

The problem and importance of scratch resistance in glass are discussed in detail by Deyrup in US. Patent 2,831,780. It is a practical industrial problem and relates to such items as the weakening of glass bottles by rubbing against each other in transit, the marring of WllldOW glass through scratches by impinging dust or glass fragments and the weakening of textile glass fibers by mutual abrasion.

In said patent, Deyrup olfers a method for overcoming this deficiency of glass by treating the glass with the vapors of a metallo-organic compound at a temperature between the lowest annealing temperature of glass and the temperature at which excessive deformation occurs. Such temperature must also be sufliciently high to cause the pyrolysis of the metallo-organic compound to form a metal oxide which melts or sublimes above the melting point of silicon dioxide, 1710 C. The oxide thus deposited produces an adherent, refractory coating, which substantially increases the scratch resistance of the surface and therefore the. practical strength of the glass.

Deyrup describes two methods for carrying out his procedure, both of which however require application of the metallo-organic compound, a titanate ester for instance, in vapor form. Such a process has inherent objections from the viewpoint of large-scale, industrial practice, such as the need for feeding a stream of inert gas containing the vaporized titanate into a heated annealing furnace, which is a process rather difiicult to control as to temperature, uniformity of feed-mixture and uniformity of coating. Also, it is rather difficult to maintain the necessary anhydrous atmosphere within the heated chamber and, at the same time, introduce and remove glass objects from the oven. The process is also wasteful, since much of the titanate material fed into the furnace coating chamber finds its way to the walls of the chamber or is hydrolyzed to a useless form.

In processes wherein various articles, including glass, have been coated with titanates for other purposes, for instance to deposit an adhesive layer on the article, it has been suggested to apply the titanate in the form of a solution thereof in an organic solvent. Such processes have the disadvantage of requiring the use of vaporizable, and therefore highly flammable, organic solvents. Also, it is difiicult to confine absolutely the vapors of the solvent, and the spreading fumes constitute a constant health hazard to the workers. Finally, some titanate esters hydrolyze readily, so unless the temperature and moisture environments of the treated glass are carefully controlled, the scratch resistance of the resulting article may be unsatisfactory.

Accordingly, it is an object of this invention to provide a process for improving the scratch resistance of glass, which shall be characterized by simplicity and general economy, uniformity of the coating applied, absence of re and health hazards, assurance against premature hydrolysis of the titanate, and other valuable, practical advantages which will appear more fully as the description proceeds.

Now, according to this invention, we select for the aforementioned treatment an aqueous-acid-soluble organic 1c V r 3,004,863

Patented Oct. 17, 1961 titanate which is characterized by stability against hydrolysis in the presence of water at ordinary temperature, and we apply said titanate to the glass from an acid aqueous solution having a pH of 2 to 5, at room temperature, prior to annealing. Selection of an aqueous solution, not only eliminates fire hazards and health hazards, but also minimizes waste and enables us to apply to the glass article a coating of any desired ultimate thickness by calculating in advance the requisite concentration of the titanate in the aqueous solution.

Following application of the solution in any convenient manner, as by rinsing, immersion or spraying, the glass body may be allowed to dry in open air: or it may be transferred directly into the annealing furnace, where it isheated, as in the Deyrup procedure, at or near the annealing temperature, but not sufficiently high to deform perceptibly the shape of the glass article. In the case of bottle glass, the heating temperature may be in the range of 510 to 670 C. With other types of glass, different temperature ranges will be selected, but these are well within the knowledge and understanding of persons skilled in this art. Thus, soft soda glass has an annealing temperature below 400 C.; borosilicate glass, near 580 C. The length of dwell in the annealing furnace will likewise follow customary practice in annealing glass, and may be of the order of a few hours.

Following annealing (or rather as part thereof) the glass is gradually cooled within the furnace atmosphere, as is customary in glass practice. But as a special further feature of this invention, the glass, following cooling, is allowed to stand in the open atmosphere for a period of at least 20 minutes (without any upper limit). This final step, which may be designated as the capping step, has an important influence on the quality of the scratch resistance protection imparted to the article. And while standing for at least 20 minutes in open air before use is apt to occur automatically with almost any article, this step takes on a positive aspect when one considers belt line production of glass articles such as milkbottles. According to our invention, we recommend holding the bottles at rest, in open air, for at least 20 minutes, before they are allowed to proceed on the conveyor belt, in order to harden so-to-speak or perfect their scratch resistance before they are exposed to the risk of rubbing against each other while in motion.

As to the chemical nature of the titanate which is to be selected according to this invention, it may be defined generally by the formula wherein R is an alkyl radicalof 2 to 4 C-atoms, y is a number whose average value is from 1 to 2, and R is a member of the group consisting of methyl, methoxy, ethyl and ethoxy. Specific illustrations of conveniently available compounds coming under the above definition are the esters (or mixtures of esters) obtainable by ester interchange reaction between 1 mole of a simple tetraalkyl titanate, for instance tetraethyl or tetraisopropyl titanate and two to three moles of an acetoacetyl compound of the formula CH CO-CH CO-R' (wherein R has the same significance as above), for instance, any of the following:

Methyl acetoacetate, CH COOH CO-OCH Ethyl acetoacetate, CH CO-CH COOC H Acetyl acetone, CH CO-CH CO-CH or Propionyl acetone, CH COCH COC H Most of the above titanate esters are known compounds, and their mode of synthesis is described more fully in British Patent No. 734,113. Since the reaction of transesterification does not necessarily replace preci sely one, two or three of the alkyl groups throughout greater than 2 are to be avoided. The preferred agents are those in which y has a single value equal to 2; but mixtures in which the average value of y is. much less than 2 are useable, if economically available. Accordingly, in the agents practically applicable for this invention, the subscript y may have an average value from Without this invention, the following example is given to illustrate our preferred mode of operation. Parts mentioned are by weight.

Example 1 A water solution of the acetyl-acetone derivative of titanium is prepared as follows:

284 parts of tetraisopropyl titanate are mixed with 200 parts of acetyl-acetone. After evolution .of heat has ceased, an orange-yellow liquid titanic acid derivative is obtained which comprises approximately 75% by weight of the acetyl-acetone derivative and 25% by weight isopropyl alcohol.

1 part of the above titanium derivative solution is mixed with 1 part of 10% acetic acid aqueous solution, and the mixture is added to 13 parts of a 50% isopropyl alcohol aqueous solution. Glass bottles are dipped into this solution. After the excess solution has been allowed to drain 7 from the bottles, they are put through an annealing lehr in which the temperature of the bottles is slowly raised from room temperature to 540 C. and then lowered to room temperature again. After standing for a short time (about minutes) exposed to air, bottles with improved scratch resistance are obtained.

As an alternative method to dipping the bottles as described above, the bottles may be sprayed with the aqueous solution of the above titanate ester.

The scratch resistance achieved can be measured by rubbing two of the treated bottles against each other. When untreated bottles-are rubbed in the same manner, they become distinctly scratched, while treated bottles are not. a

. On a laboratory scale, a convenient method for testing the scratch resistance imparted to glass by any given titanate ester composition is as follows:

A drop of the titanate solution to be tested is placed on a clean glass microscope slide, and is spread out by the aid of another glass slide to cover just about one half of the first slide. Theother half then remains as a control, The slide is then dried, annealed, cooled and allowed to stand in open air for 20 minutes or more, as in the example above.

When the edge of an untreated slide is then drawn over the treated slidelengthwise, starting from the untreated half, a scratch is produced which terminates abruptly as the boundary of the treated portion is crossed.

Ina similar manner'the ester-interchange product of 1 mole of tetraisopropyl, tetrabutyl or tetraethyl titanate with 3 moles of acetyl-acetone or with 2 to '3 moles of methyl or ethyl acetoacetate. may be prepared and applied to glass, with the same results.

In lieu of acetic acid in the treatment bath any other convenient acid may be employed to achieve a pH range between 2 to 5, for instance hydrochloric .or sulfuric.

The isopropyl alcohol used in the treatment bath in the above example has as its function to facilitate/solution of the titanateester. Ethyl alcohol or methyl alcohol may be used in its place. lfa stronger acid than acetic 4 a is employed, the quantity of alcohol may be considerably reduced, up to the point of total elimination.

It will be understood that the details of procedure above set forth may be varied widely the skill of those engaged in'this art. The following additional details will assist in the understanding and control of the invention. 7

As already mentioned, the thickness of the eventual coating can be controlled by selecting the proper concentration for the applied aqueous solution. This selection can be eifected. on the basis of an experience chart which correlates the thickness of the final film on the glass in a few cases to the concentrations of the solutions applied in the respective cases. The needed concentration of the solution for any other' specified eventual thickness of coating may then be calculated by interpolation of extrapolation in the experience chart.

Desirable thicknesses in the ultimate dry coating are from about 5 to aboutl0O millimicrons. When the coating exceeds 100 millimicrons in thickness, the scratch resistance begins to drop off.

The thicknms of the final coating may be gauged or judged by various means. Thus, with ordinary white light, a coating thicker than 100 millimicrons will show colored diffraction efiects.

The nature of the coating and the cause of the scratch resistance observed are only partially understood. The surface coatingsproduced are known to be amorphous when less than 100 .millimicrons thick; that is, they have no regular crystallinecharacteristics. On the other hand, coatings thickerthan 100 millirnicrons start to show a crystalline X-ray pattern, which is characteristic of the titanium dioxide mineral anatase.

The method of bonding to the glass surface is not known but is surmised to involve TiO--Si bonding.

Glass treated according to this invention is not diiferent in appearance from untreated glass of the same type. But the two can be distinguished by special physical tests. Thus, the coeflicient of friction of untreated glass is about 0.8 to 0.9, while that of the treated glass has been found to be about 0.17 to 0.25.

In certain instances, particularly when the compositions prepared'from methyl or ethyl acetoacetate and tetrabutyl titanate (acidified with mineral acids and containing no added alcohol) are usedin this invention, complete wetting of the glass surface may be difiicult to obtain. If this occurs, the addition of a small amount of a wetting agent which is stableto acidic conditions overcomes the diificulty. Useful wetting agents for this purpose are the nonionic condensation products of longchain fatty alcohols, e.-g. octadecyl alcohol, with from 4 to 20 moles "of ethylene oxide.

. r We claim as our invention:

the formula wherein R is an alkyl radical of 2 to 4 C-atoms, y is a number of average value from 1 to 2, and R' is a member of the group consisting of methyl, ethyl, methoxy and ethoxy. f

2.'A process as in claim 1, wherein the temperature in the heating step'is between 510 and 670 C.

3. The process as in claim 1, wherein y in the formula of the titanate ester hasan average value of about 2.

4. A process of increasing the scratch resistance of a glass body, which comprises applying to the surface of said body an acid aqueous solution of a titanate ester composition of the formula wherein R is an alkyl radical of 2 to 4 C-atoms, y is a number of average value from 1 to 2, and R is a member of the group consisting of methyl, ethyl, methoxy and ethoxy, said solution having a pH value between 2 and 5, allowing the excess moisture to drain, subjecting the treated glass to heating at a temperature suflicient to anneal the glass but below that at which perceptible deformation of the shape of the glass body steps in, cooling the glass body and allowing the same to stand in open air for not less than 20 minutes before exposing the same to handling wherein rubbing of the glass body against other glass bodies is likely to occur.

5. A process of endowing glass bottles with increased resistance to scratching by mutual rubbing in transit, which comprises treating the outer surface of said bottles with an aqueous solution, at pH 2 to 5, of a titanate ester composition of the formula (RO) Ti(OC|3=CH-fil-R')4- wherein R is an alkyl radical of 2 to 4 C-atoms, y is a number of average value from 1 to 2, and R is a member of the group consisting of methyl, ethyl, methoxy and ethoxy, exposing the bottles to annealing heat at a 7. A process as in claim 5, wherein the titanate ester composition employed consists essentially of the compound of formula (CQH1O)lTi(O( J=GHfi-OCans 8. A process as in claim 5, wherein the titanate ester composition employed consists essentially of the compound of formula References Cited in the file of this patent UNITED STATES PATENTS 2,680,108 Schmidt June 1, 1954 2,768,909 Haslam Oct. 30, 1956 2,831,780 Deyrup Apr. 22, 1958

Patent Citations
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US2768909 *Jul 28, 1953Oct 30, 1956Du PontMethod of coating surface with transparent film and product resulting therefrom
US2831780 *Apr 21, 1955Apr 22, 1958Du PontMethod for improving the scratch resistance and strength of glass articles
Referenced by
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US3130071 *Mar 23, 1961Apr 21, 1964Du PontProcess for increasing the scratch resistance of glass by treatment with titanium lactate polymer
US3161534 *Dec 22, 1961Dec 15, 1964Du PontProcess for increasing the scratch resistance of glass
US3161535 *Dec 22, 1961Dec 15, 1964Du PontProcess for increasing the scratch resistance of glass
US3161536 *Dec 22, 1961Dec 15, 1964Du PontProcess for increasing the scratch resistance of glass
US3161537 *Dec 22, 1961Dec 15, 1964Du PontProcess for increasing the scratch resistance of glass
US3182839 *Mar 29, 1963May 11, 1965American Can CoGlass container
US3226249 *Sep 11, 1961Dec 28, 1965Philips CorpMethod of providing light diffusing coatings on quartz and quartz objects provided with such coatings
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U.S. Classification65/30.1, 65/117, 556/10, 215/12.2, 427/384, 427/374.1, 556/40, 427/8, 65/60.3, 556/7
International ClassificationC03C17/25
Cooperative ClassificationC03C17/256, C03C2217/212, C03C2218/112, C03C2218/111
European ClassificationC03C17/25C